(Z)-Hex-2-ene, 5-methyl-

Details

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Internal ID 4aa2b423-b361-4991-92f6-9a406ac1eee4
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Unsaturated aliphatic hydrocarbons
IUPAC Name (Z)-5-methylhex-2-ene
SMILES (Canonical) CC=CCC(C)C
SMILES (Isomeric) C/C=C\CC(C)C
InChI InChI=1S/C7H14/c1-4-5-6-7(2)3/h4-5,7H,6H2,1-3H3/b5-4-
InChI Key GHBKCPRDHLITSE-PLNGDYQASA-N
Popularity 9 references in papers

Physical and Chemical Properties

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Molecular Formula C7H14
Molecular Weight 98.19 g/mol
Exact Mass 98.109550447 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.61
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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cis-5-Methyl-2-hexene
13151-17-2
(Z)-5-methylhex-2-ene
(Z)-5-Methyl-2-hexene
POQ2TVS2I5
5-Methyl-2-hexene, (2Z)-
2-Hexene, 5-methyl-, (Z)-
2-Hexene, 5-methyl-, (2Z)-
(Z)-(CH3)2CHCH2CH=CHCH3
Z-5-methyl-2-hexene
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of (Z)-Hex-2-ene, 5-methyl-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9928 99.28%
Caco-2 + 0.7581 75.81%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Lysosomes 0.3573 35.73%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8791 87.91%
OATP1B3 inhibitior + 0.9468 94.68%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9315 93.15%
P-glycoprotein inhibitior - 0.9842 98.42%
P-glycoprotein substrate - 0.9720 97.20%
CYP3A4 substrate - 0.7619 76.19%
CYP2C9 substrate - 0.8071 80.71%
CYP2D6 substrate - 0.7561 75.61%
CYP3A4 inhibition - 0.9736 97.36%
CYP2C9 inhibition - 0.9354 93.54%
CYP2C19 inhibition - 0.9457 94.57%
CYP2D6 inhibition - 0.9283 92.83%
CYP1A2 inhibition - 0.8494 84.94%
CYP2C8 inhibition - 0.9926 99.26%
CYP inhibitory promiscuity - 0.8361 83.61%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6183 61.83%
Carcinogenicity (trinary) Non-required 0.4703 47.03%
Eye corrosion + 0.9809 98.09%
Eye irritation + 0.9928 99.28%
Skin irritation + 0.9089 90.89%
Skin corrosion - 0.8073 80.73%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5832 58.32%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.7463 74.63%
skin sensitisation + 0.9232 92.32%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity - 0.9667 96.67%
Mitochondrial toxicity + 0.8750 87.50%
Nephrotoxicity - 0.5646 56.46%
Acute Oral Toxicity (c) III 0.7963 79.63%
Estrogen receptor binding - 0.9841 98.41%
Androgen receptor binding - 0.9240 92.40%
Thyroid receptor binding - 0.9226 92.26%
Glucocorticoid receptor binding - 0.9282 92.82%
Aromatase binding - 0.9018 90.18%
PPAR gamma - 0.9553 95.53%
Honey bee toxicity - 0.8959 89.59%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9465 94.65%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL1907 P15144 Aminopeptidase N 86.75% 93.31%
CHEMBL2581 P07339 Cathepsin D 86.62% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.20% 96.09%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Citrus × aurantium
Citrus deliciosa

Cross-Links

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PubChem 5364850
NPASS NPC137472